Canonical Allele Identifier: CA2622478661
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924847-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924847A>G , CM000675.2:g.27924847A>G GRCh38
NC_000013.10:g.28498984A>G , CM000675.1:g.28498984A>G GRCh37
NC_000013.9:g.27396984A>G NCBI36
NG_008183.1:g.9817A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*146A>G MANE Select ENSP00000370421.4:n.*146A>G
ENST00000381033.4:c.*146A>G ENSP00000370421.4:n.*146A>G
NM_000209.3:c.*146A>G NP_000200.1:n.*146A>G
NM_000209.4:c.*146A>G MANE Select NP_000200.1:n.*146A>G
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